Items where Author is "Rokach, O."

Yes

Rokach, O. and Sekulic-Jablanovi, M. and Voermans, N. and Wilmhurst, J. and Pillay, K. and Heytens, L. and Zhou, H. and Muntoni, F. and Gautel, M. and Nevo, Y. and Mitrani-Rosenbaum, S. and Attali, R. and Finotti, A. and Gambari, R. and Mosca, B. and Jungbluth, H. and Zorzato, F. and Treves, S.. (2015) Epigenetic changes as a common trigger of muscle weakness in congenital myopathies. Human Molecular Genetics, 24. pp. 4636-4647.

Rokach, O. and Ullrich, N. D. and Rausch, M. and Mouly, V. and Zhou, H. and Muntoni, F. and Zorzato, F. and Treves, S.. (2013) Establishment of a human skeletal muscle-derived cell line : biochemical, cellular and electrophysiological characterization. Biochemical Journal , 455 (2). pp. 169-177.

Zhou, H. and Rokach, O. and Feng, L. and Munteanu, I. and Mamchaoui, K. and Wilmshurst, J. M. and Sewry, C. and Manzur, A. Y. and Pillay, K. and Mouly, V. and Duchen, M. and Jungbluth, H. and Treves, S. and Muntoni, F.. (2013) RyR1 Deficiency in Congenital Myopathies Disrupts Excitation–Contraction Coupling. Human Mutation, 34 (7). pp. 986-996.

Attali, R. and Aharoni, S. and Treves, S. and Rokach, O. and Becker Cohen, M. and Fellig, Y. and Straussberg, R. and Dor, T. and Daana, M. and Mitrani-Rosenbaum, S. and Nevo, Y.. (2013) Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation. PLoS one, 8 (7). e69296.